| Tag | Content |
|---|
EnhancerAtlas ID | HS129-22032 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr20:14966540-14967390 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr20:14966958-14966973 | AGTTAATGAATAACC | + | 6.14 | | MSC | MA0665.1 | chr20:14966748-14966758 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr20:14966748-14966758 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr20:14966748-14966758 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr20:14966748-14966758 | AACAGCTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35330 | chr20:14963816-14968794 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I014984 | chr20 | 14965084 | 14968669 |
|
Enhancer Sequence | TTCCAAAGTG CTGGGATTAC AGGTGTGAGC CACCTTGCCC TGCAGAAATA CCAATTATTA 60
AAAACTCAGA GGTTGTAGTG CAACATATTT GGGAGTGGTC ACACCCCATG GCCTTTGATT 120
TTAGTCTGAA GATTGAAAAT AACCTTTGGA TTTTACCTTG ACAAGGAAGT TGTTCCTCAG 180
TGGACACAGA CATCATAGTT GGCATAGAAA CAGCTGTTGG GTTATTCCTG GGCCATTGAA 240
GACATGGCAC CTGGCCCAGT CTGAATGGTT GTTCTCTCCT GGTTGCTTGT TTAAATAAAG 300
GTTAAGCAAA AATTCTTTTT TGGTTTTGAT TTCAGGAAGA AATAAGGGAG TGACTGCAAT 360
GTTATCTGAA AATGAGCATT TCCTGTTTCC TCAGGCATTT CTTTATGACC CCCATTAAAG 420
TTAATGAATA ACCAAGTGTC TGACACAGTT GAGCGTAATA TGCCTCACCT AAGGTTCCCG 480
GTGGCTGCAC ATTTTTGTGG GAAATGACCT TCAGTTCCTG CAGATCCATT ATTAGGCAAT 540
CTCTTAGTTA TAGACTTTAT CTTCCCAAAA CATTCAAATC ACATATTAGC CAAATCACTT 600
AGATACCGTC CTAAGTGCTG GAACTCTTTA AGTCTTGTTA GCAGAAAAGG CTAAAGTTTA 660
GGTAAATAAG CAGATCTGTT CCACAAATGA TTCCTCACCT TAGGTATTTA TGAAAAAGCT 720
CTGATAAACT TTTGAAAGCA GAAAAAGACG TTAAAAAATC TTACTGTGAG CCTGAAAACA 780
TAAACATAAA TCAGCTAAAA GATAATTTGC CTTAATAGGT AGTGGGCGAT GGGGGAGGAG 840
AGTGATCAGG 850
|
